EMGALITY is a Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is Galcanezumab.
Product ID | 0002-1436_4b767820-97fe-430d-8e77-6047e82ac81e |
NDC | 0002-1436 |
Product Type | Human Prescription Drug |
Proprietary Name | EMGALITY |
Generic Name | Galcanezumab-gnlm |
Dosage Form | Injection, Solution |
Route of Administration | SUBCUTANEOUS |
Marketing Start Date | 2018-09-27 |
Marketing Category | BLA / BLA |
Application Number | BLA761063 |
Labeler Name | Eli Lilly and Company |
Substance Name | GALCANEZUMAB |
Active Ingredient Strength | 120 mg/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2018-09-27 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA761063 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-09-27 |
Marketing End Date | 2018-09-27 |
Marketing Category | BLA |
Application Number | BLA761063 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2018-09-27 |
Marketing Category | BLA |
Application Number | BLA761063 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-09-27 |
Marketing Category | BLA |
Application Number | BLA761063 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2018-09-27 |
Ingredient | Strength |
---|---|
GALCANEZUMAB | 120 mg/mL |
SPL SET ID: | 33a147be-233a-40e8-a55e-e40936e28db0 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0002-1436 | EMGALITY | galcanezumab-gnlm |
0002-2377 | EMGALITY | galcanezumab-gnlm |
0002-3115 | EMGALITY | galcanezumab-gnlm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EMGALITY 88112647 not registered Live/Pending |
Eli Lilly and Company 2018-09-11 |
EMGALITY 87435081 5633683 Live/Registered |
Eli Lilly and Company 2017-05-03 |
EMGALITY 87263356 5628446 Live/Registered |
Eli Lilly and Company 2016-12-09 |